C. Ronald Scott

6.9k total citations · 2 hit papers
81 papers, 4.7k citations indexed

About

C. Ronald Scott is a scholar working on Physiology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, C. Ronald Scott has authored 81 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Physiology, 30 papers in Pediatrics, Perinatology and Child Health and 26 papers in Clinical Biochemistry. Recurrent topics in C. Ronald Scott's work include Lysosomal Storage Disorders Research (43 papers), Neonatal Health and Biochemistry (28 papers) and Metabolism and Genetic Disorders (26 papers). C. Ronald Scott is often cited by papers focused on Lysosomal Storage Disorders Research (43 papers), Neonatal Health and Biochemistry (28 papers) and Metabolism and Genetic Disorders (26 papers). C. Ronald Scott collaborates with scholars based in United States, Canada and Australia. C. Ronald Scott's co-authors include Laurence A. Harker, Russell Ross, Michael H. Gelb, František Tureček, S. J. Slichter, Sherrill J. Slichter, Martin Sadı́lek, Joel Charrow, Yijun Li and Néstor Chamoles and has published in prestigious journals such as Science, New England Journal of Medicine and The Lancet.

In The Last Decade

C. Ronald Scott

79 papers receiving 4.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Homocystine-induced arteriosclerosis. The role of endothelial cell injury and platelet response in its genesis.

1976 757 citations C. Ronald Scott et al. profile →
Homocystinemia

1974 542 citations C. Ronald Scott et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C. Ronald Scott United States	36	2.2k	1.3k	931	856	826	81	4.7k
Joe T.R. Clarke Canada	38	2.6k 1.2×	689 0.5×	1.5k 1.6×	1.1k 1.3×	696 0.8×	84	4.5k
Seymour Packman United States	44	2.1k 0.9×	879 0.7×	2.6k 2.8×	854 1.0×	1.2k 1.5×	135	6.5k
Melissa Wasserstein United States	35	1.9k 0.8×	529 0.4×	1.4k 1.5×	354 0.4×	840 1.0×	93	3.3k
Barbara K. Burton United States	50	3.2k 1.4×	1.3k 1.0×	2.9k 3.2×	1.0k 1.2×	2.8k 3.4×	248	7.7k
John J. Mitchell United States	33	1.2k 0.5×	575 0.4×	1.7k 1.9×	402 0.5×	1.0k 1.2×	131	4.2k
Alberto Burlina Italy	49	2.8k 1.2×	1.5k 1.2×	3.9k 4.2×	466 0.5×	4.5k 5.5×	234	8.0k
Leonard Laster United States	29	1.1k 0.5×	1.1k 0.8×	1.3k 1.4×	541 0.6×	765 0.9×	55	3.9k
Carlo Dionisi‐Vici Italy	50	1.7k 0.8×	1.5k 1.1×	4.9k 5.3×	587 0.7×	4.6k 5.6×	292	9.3k
Pietro Strisciuglio Italy	30	532 0.2×	442 0.3×	1.1k 1.1×	411 0.5×	597 0.7×	131	2.9k
Soumeya Bekri France	29	788 0.4×	318 0.2×	1.2k 1.3×	676 0.8×	293 0.4×	124	3.4k

Countries citing papers authored by C. Ronald Scott

Since Specialization

Citations

This map shows the geographic impact of C. Ronald Scott's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by C. Ronald Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Ronald Scott more than expected).

Fields of papers citing papers by C. Ronald Scott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Ronald Scott. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by C. Ronald Scott. The network helps show where C. Ronald Scott may publish in the future.

Co-authorship network of co-authors of C. Ronald Scott

This figure shows the co-authorship network connecting the top 25 collaborators of C. Ronald Scott. A scholar is included among the top collaborators of C. Ronald Scott based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Ronald Scott. C. Ronald Scott is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Scott, C. Ronald, et al.. (2025). Lemierre Disease: The Unexpected Thromboembolic Complication of a Sore Throat. American Journal of Respiratory and Critical Care Medicine. 211(Supplement_1). A3937–A3937.

Lee, Christine K., et al.. (2025). A Cross-Sectional Retrospective Review of Neuropsychiatric Comorbidities in Children With Non-Alcoholic Fatty Liver Disease. Clinical Pediatrics. 64(9). 1274–1280. 1 indexed citations

Jack, Rhona M. & C. Ronald Scott. (2019). Validation of a therapeutic range for nitisinone in patients treated for tyrosinemia type 1 based on reduction of succinylacetone excretion. JIMD Reports. 46(1). 75–78. 9 indexed citations

Hong, Xinying, Arun Kumar, C. Ronald Scott, & Michael H. Gelb. (2018). Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkers. Molecular Genetics and Metabolism. 124(2). 101–108. 5 indexed citations

Gelb, Michael H., C. Ronald Scott, František Tureček, & Hsuan-Chieh Liao. (2017). Comparison of tandem mass spectrometry to fluorimetry for newborn screening of LSDs. Molecular Genetics and Metabolism Reports. 12. 80–81. 8 indexed citations

Elliott, Susan, Norman E. Buroker, Jason J. Cournoyer, et al.. (2016). Pilot study of newborn screening for six lysosomal storage diseases using Tandem Mass Spectrometry. Molecular Genetics and Metabolism. 118(4). 304–309. 128 indexed citations

Kumar, Arun, Zdeněk Spáčil, Farideh Ghomashchi, et al.. (2015). Fluorimetric assays for N-acetylgalactosamine-6-sulfatase and arylsulfatase B based on the natural substrates for confirmation of mucopolysaccharidoses types IVA and VI. Clinica Chimica Acta. 451(Pt B). 125–128. 10 indexed citations

Scott, C. Ronald, et al.. (2013). Quantification of sulfatides in dried blood and urine spots from metachromatic leukodystrophy patients by liquid chromatography/electrospray tandem mass spectrometry. Clinica Chimica Acta. 433. 39–43. 22 indexed citations

Spáčil, Zdeněk, et al.. (2011). Comparative Triplex Tandem Mass Spectrometry Assays of Lysosomal Enzyme Activities in Dried Blood Spots Using Fast Liquid Chromatography: Application to Newborn Screening of Pompe, Fabry, and Hurler Diseases. Analytical Chemistry. 83(12). 4822–4828. 34 indexed citations

10.

Tarini, Beth A., Wylie Burke, C. Ronald Scott, & Benjamin S. Wilfond. (2008). Waiving informed consent in newborn screening research: Balancing social value and respect. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 148C(1). 23–30. 27 indexed citations

11.

Tureček, František, C. Ronald Scott, & Michael H. Gelb. (2007). Tandem Mass Spectrometry in the Detection of Inborn Errors of Metabolism for Newborn Screening. Methods in molecular biology. 359. 143–157. 19 indexed citations

12.

Yu, Chunli & C. Ronald Scott. (2006). Human biochemical genetics: An insight into inborn errors of metabolism. Journal of Zhejiang University SCIENCE B. 7(2). 165–166. 1 indexed citations

13.

Jack, Rhona M., et al.. (2006). The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease. Genetics in Medicine. 8(5). 307–312. 36 indexed citations

14.

Scott, C. Ronald. (2006). The genetic tyrosinemias. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 142C(2). 121–126. 122 indexed citations

15.

Andersson, Hans C., Joel Charrow, Paige Kaplan, et al.. (2005). Individualization of long-term enzyme replacement therapy for Gaucher disease. Genetics in Medicine. 7(2). 105–110. 89 indexed citations

16.

Charrow, Joel, Joan A. Esplin, Paige Kaplan, et al.. (1999). Recommendations for Diagnosis, Evaluation, and Monitoring of Patients With Gaucher Disease. JAMA Internal Medicine. 159(11). 1255–1255. 1 indexed citations

17.

Charrow, Joel, Joan A. Esplin, T. John Gribble, et al.. (1998). Gaucher Disease. Archives of Internal Medicine. 158(16). 1754–1754. 110 indexed citations

18.

Sharar, Sam R., Charles M. Haberkern, Rhona M. Jack, & C. Ronald Scott. (1991). Anesthetic Management of a Child With Methylmalonyl-Coenzyme A Mutase Deficiency. Anesthesia & Analgesia. 73(4). 499???501–499???501. 11 indexed citations

19.

Keens, Thomas G., et al.. (1981). Gastro esophageal reflux prevents recovery from broncho pulmonary dysplasia. Clinical research. 29(1). 149. 4 indexed citations

20.

Scott, C. Ronald, Jean I. Bryant, & C. Benjamin Graham. (1971). A new craniodigital syndrome with mental retardation. The Journal of Pediatrics. 78(4). 658–663. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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